Company:
Katalyst Healthcares & Life Sciences
Location: Chicago
Closing Date: 28/10/2024
Salary: £125 - £150 Per Annum
Hours: Full Time
Type: Permanent
Job Requirements / Description
Responsibilities:
- Responsible for supporting the Programming deliveries of a clinical study or project.
- Implements statistical programming aspects of the protocol and the clinical development program
- Ensures high quality is built into own deliverables and the quality delivered by other programmers
- Programs independently with high efficiency and quality
- Writes and/or implements specifications and oversees completeness of relevant documentation
- Contribute to the development of best practice to improve quality, efficiency and effectiveness within function
- Ensures compliance with standards and automation usage
- Plans and support team activities and tasks
- Communicates and escalates risks within the assigned studies and/or projects
- Works proactively with study team members including but not limited to the Statistician, Lead Programmer, Data Manager and Study Leader.
Requirements:
- Bachelor's degree in computer science (CS), statistics or related scientific disciplines with 7 yrs. clinical programming (CDISC) experience; Master's degree in CS, statistics or related disciplines with 5 yrs. of clinical programming (CDISC) experience.
- Require strong Oncology TA with experience in ISS & Client.
- Experience in blood cancer and the Lugano criteria is a plus.
- Excellent programming skills including macro language.
- Ability to proactively manage concurrent activities within a study or part of project.
- Proficient knowledge of the clinical development process.
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Katalyst Healthcares & Life Sciences
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